Inelastic electron tunneling spectroscopy for probing strongly correlated many-body systems by scanning tunneling microscopy

Medientyp: E-Artikel

Titel: Inelastic electron tunneling spectroscopy for probing strongly correlated many-body systems by scanning tunneling microscopy

Beteiligte: Eickhoff, Fabian [VerfasserIn]; Kolodzeiski, Elena [VerfasserIn]; Esat, Taner [VerfasserIn]; Fournier, Norman [VerfasserIn]; Wagner, Christian [VerfasserIn]; Deilmann, Thorsten [VerfasserIn]; Temirov, Ruslan [VerfasserIn]; Rohlfing, Michael [VerfasserIn]; Tautz, F. Stefan [VerfasserIn]; Anders, Frithjof B. [VerfasserIn]

Erschienen: Inst., 2020

Sprache: Englisch

DOI: https://doi.org/10.1103/PhysRevB.101.125405

ISSN: 1094-1622; 0556-2805; 1550-235X; 1050-2947; 1098-0121; 0163-1829; 1095-3795; 2469-9969; 1538-4489; 2469-9950

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Beschreibung: We present an extension of the tunneling theory for scanning tunneling microscopy (STM) to include different types of electron-vibrational couplings responsible for inelastic contributions to the tunnel current in the strong-coupling limit. It allows for a better understanding of more complex scanning tunneling spectra of molecules on a metallic substrate in separating elastic and inelastic contributions. The starting point is the exact solution of the spectral functions for the electronically active local orbitals in the absence of the STM tip. This includes electron-phonon coupling in the coupled system comprising the molecule and the substrate to arbitrary order including the antiadiabatic strong-coupling regime as well as the Kondo effect on a free-electron spin of the molecule. The tunneling current is derived in second order of the tunneling matrix element which is expanded in powers of the relevant vibrational displacements. We use the results of an ab initio calculation for the single-particle electronic properties as an adapted material-specific input for a numerical renormalization group approach for accurately determining the electronic properties of a 1,4,5,8-naphthalene-tetracarboxylic acid dianhydride molecule on Ag(111) as a challenging sample system for our theory. Our analysis shows that the mismatch between the ab initio many-body calculation of the tunnel current in the absence of any electron-phonon coupling to the experimental scanning tunneling spectra can be resolved by including two mechanisms: (i) a strong unconventional Holstein term on the local substrate orbital leads to the reduction of the Kondo temperature and (ii) a further electron-vibrational coupling to the tunneling matrix element is responsible for inelastic steps in the dI/dV curve at finite frequencies

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